Allele Registry

Canonical Allele Identifier: PA915956970

Gene: CP HGNC NCBI

ClinVar RCV:

RCV000496150

RCV003226310

ClinVar Variation:

431113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000087.2:p.Leu919Pro	CA354929700 NM_000096.4:c.2756T>C